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American Journal of Medical Genetics|February 1, 1991
Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27-q28B A Oostra, D F Majoor-Krakauer, J O van Hemel, et al.American Journal of Medical Genetics|September 1, 1991
DNA analysis in patients with lissencephaly type I and other cortical dysplasiasB A Oostra, J F de Rijk-van Andel, H J Eussen, et al.Nature Genetics|February 1, 1997
Characterization of the full fragile X syndrome mutation in fetal gametesH E Malter, J C Iber, R Willemsen, et al.BJOG : an International Journal of Obstetrics and Gynaecology|July 10, 2007
STOX1 gene in pre-eclampsia and intrauterine growth restrictionA L Berends, A M Bertoli-Avella, C J M de Groot, et al.Neurobiology of Aging|October 1, 2011
Plasma β amyloid and the risk of Alzheimer's disease in Down syndromeAntonia M W Coppus, Maaike Schuur, Jeanet Vergeer, et al.Nature Genetics|November 1, 1994
Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXEJ E Parrish, B A Oostra, A J Verkerk, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 11, 2011
Fragile X mental retardation protein regulates new neuron differentiation in the adult olfactory bulbSophie Scotto-Lomassese, Antoine Nissant, Tatiana Mota, et al.Genomics|January 1, 1993
Isolation and characterization of 25 unique DNA markers for human chromosome 22N A van Biezen, R H Lekanne Deprez, A Thijs, et al.American Journal of Medical Genetics|February 1, 1991
New polymorphism and a new chromosome breakpoint establish the physical and genetic mapping of DXS369 in the DXS98-FRAXA intervalI Oberlé, A Vincent, N Abbadi, et al.Neurobiology of Disease|May 26, 2009
Ultrastructural analysis of the functional domains in FMRP using primary hippocampal mouse neuronsJosien Levenga, Ronald A M Buijsen, Maria Rifé, et al.Pageof 51